Article
Robust Visible Light Photoswitching with Ortho-Thiol Substituted Azobenzenes
Chemical Communications
Document Type
Article
Publication Date
1-1-2013
Subjects
- Azo compounds -- Absorption,
- Photochemistry,
- Nanostructured materials
Disciplines
Abstract
Introduction of S-ethyl groups in all four ortho positions of azobenzene prevents reduction of the azo group by intracellular glutathione, while enhancing the absorptivity to ∼10000 M−1 cm−1 in the blue and green regions of the visible spectrum. cis-to-trans isomerization occurs thermally on the minutes timescale. Further, this substitution pattern permits switching with red light, a color that is more penetrating through biological tissues than other parts of the visible spectrum.
DOI
10.1039/c3cc46045b
Persistent Identifier
http://archives.pdx.edu/ds/psu/16178
Citation Information
Samanta, S.; McCormick, T. M.; Schmidt, S. K.; Seferos, D. S.; Woolley, G. A. “Robust visible light photoswitching with ortho-thiol substituted azobenzenes” Chemical Communications. 49 (87), 10314-10316, 2013.
This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. Open Access
This journal is © The Royal Society of Chemistry 2013
*At the time of publication Theresa M. McCormick was affiliated with University of Toronto.